首页> 外文期刊>JAMA: the Journal of the American Medical Association >Screening newborns for congenital cytomegalovirus infection.
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Screening newborns for congenital cytomegalovirus infection.

机译:筛查新生儿先天性巨细胞病毒感染。

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However, 2 challenges confront universal screening for congenital CMV infection. First, universal screening is only justified when an effective intervention exists that prevents adverse health outcomes, such as averting intellectual disability when infants who lack phenylalanine hy-droxylase initiate a diet low in phenylalanine early in life. At present, no such solution exists for CMV. Although neonatal ganciclovir therapy improves hearing outcomes in some infants,7 the benefits are not universal and the risk/benefit ratio of ganciclovir therapy in infants with silent congenital CMV infection has not been sufficiently well-established to recommend such therapy for all CMV-infected infants. Nonetheless, knowing which infants are infected with CMV has benefit through early identification of infants at risk of CMV-induced hearing loss and may have additional benefits in the future when new and more effective antiviral strategies become available.
机译:然而,对先天性巨细胞病毒感染的普遍筛查面临两个挑战。首先,只有在存在能够防止不良健康后果的有效干预措施时(例如,当缺乏苯丙氨酸羟化酶的婴儿在生命初期就开始摄入低苯丙氨酸的饮食时)避免智力残疾时,才可以进行普遍筛查。目前,CMV不存在这样的解决方案。尽管新生儿更昔洛韦治疗可改善某些婴儿的听力结果,[7]但这种益处并不普遍,对于尚无先天性CMV感染的婴儿,更昔洛韦治疗的风险/获益比还没有得到充分确立,无法向所有CMV感染的婴儿推荐这种治疗。但是,通过早期识别处于CMV诱发的听力损失风险中的婴儿,知道哪些婴儿感染了CMV会有所帮助,并且在将来出现新的更有效的抗病毒策略时,可能会带来其他好处。

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